At Firstmed, medicine safety assessment begins in the research laboratory, and continues for as long as a medicine is prescribed to patients anywhere in the world. This process detailed below is our science-based processes we follow when we receive a report of an adverse event.

Firstmed, first runs the adverse event report through its process and then if merits are found reports to FDA and all worldwide regulatory organizations. Please send any adverse events to medwatch@firstmedpharma.com